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Prognostic variables in oligodendroglial tumors: a single-institution study of 95 cases

机译:少突胶质细胞瘤的预后变量:单机构研究95例

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摘要

We analyzed the relationships among clinical variables, histology, 1p/19q status, and outcome in 95 patients with oligodendroglial tumors.The study enrolled adult patients who underwent first-time surgery for a supratentorial oligodendroglial tumor at Oslo University Hospital, Rikshospitalet. Tumors were: 27 oligodendrogliomas, WHO grade II; 32 oligoastrocytomas, WHO grade II; 16 anaplastic oligodendrogliomas, WHO grade III; 14 anaplastic oligoastrocytomas, WHO grade III; and 6 glioblastomas with a major oligodendroglial component, WHO grade IV. The clinical files were reviewed. Three neuropathologists evaluated the histological slides independently. Loss-of-heterozygosity analysis for 1p and 19q was performed by PCR.Favorable prognostic factors from univariate analyses included seizures as presenting symptom, female sex, location in the frontal lobe, low WHO grade, classic histology, absence of gemistocytic cells, and combined 1p/19q loss. Solitary 19q loss was a negative prognostic marker. 1p/19q status was of prognostic significance in both tumors with classic and nonclassic oligodendroglial histology. In the multivariate analysis, WHO grade II (P< .001), frontal tumor location (P= .002), and combined 1p/19q loss (P< .001) remained favorable prognostic variables.Our results suggest that tumor location, WHO grade, and 1p/19q status are important independent variables associated with survival in oligodendroglial tumors. The study suggests that solitary 19q loss is a negative prognostic variable and that 1p/19q loss is associated with prolonged survival also in oligodendroglial tumors without classic histology.
机译:我们分析了95例少突神经胶质瘤患者的临床变量,组织学,1p / 19q状态和结局之间的关系。该研究招募了在Rikshospitalet的奥斯陆大学医院首次接受了幕上少突神经胶质瘤手术的成年患者。肿瘤为:27例世界卫生组织II级少突胶质细胞瘤。世界卫生组织II级32个少体星形细胞瘤;世界卫生组织III级16例间变性少突胶质细胞瘤;世卫组织三级14个间变性少星形细胞瘤;以及6个具有主要少突神经胶质成分的胶质母细胞瘤,世卫组织IV级。临床文件进行了审查。三位神经病理学家独立评估了组织切片。通过PCR对1p和19q进行杂合丧失分析。单因素分析的有利预后因素包括发作,症状,女性,额叶位置,WHO分级低,经典组织学,缺乏双核细胞,以及合并1p / 19q损失。单独的19q丢失是阴性的预后指标。 1p / 19q状态在具有经典和非经典性少突神经胶质组织学的肿瘤中均具有预后意义。在多变量分析中,WHO II级(P <.001),额部肿瘤位置(P = .002)和合并1p / 19q丢失(P <.001)仍是有利的预后变量。等级和1p / 19q状态是与少突神经胶质瘤生存相关的重要独立变量。该研究表明,在没有经典组织学的情况下,少突胶质细胞瘤中单独的19q丢失是负的预后变量,并且1p / 19q丢失也与延长的生存期相关。

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